- Bristol Myers Squibb (Devens, MA)
- … CMC deliverables, technical team objectives, life-cycle improvements, and regulatory commitments. + Provides technical quality expertise and compliance oversight ... . **Position Summary** Bristol-Myers Squibb is seeking an Associate Director , Principal Product Quality Leader (PQL), in Global Product Quality… more
- Lilly (Indianapolis, IN)
- …+ Ensure process definition of critical parameters are in alignment with regulatory submission. + Ensure that each of the department and external partner ... operate in compliance with cGMPs, regulatory commitments and Lilly Functional Standards though appropriate oversight....plan (BP), cGMPs and internal standards. + Escalate to Sr . Management in a timely fashion risks to supply,… more
- Mallinckrodt Pharmaceuticals (Horsham, PA)
- Job Title Associate Director , Manufacturing Operations Requisition JR000015470 Associate Director , Manufacturing Operations (Open) Location Horsham, PA ... Additional Locations Job Description Summary Job Description The Associate Director , Manufacturing Operations will provide leadership and management of operations at… more
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …+ Other duties as assigned related to CMC workstream as directed by CMC technical director . **Who is USP Looking For?** The successful candidate will have ... work environment. **Brief Job Overview** USP is seeking a Senior Technical Advisor, Pharmaceutical Formulation and Manufacturing Strategy with strengthening… more
- J&J Family of Companies (Spring House, PA)
- …+ Drive effective communication and cross‑functional collaboration with R/D Clinical, Regulatory , Pharmacokinetics, CMC , Quality Assurance, and Data Management ... Description:** **We are searching for the best talent for our Associate Director , Bioanalysis position located in Spring House, PA.** **About Innovative Medicine**… more
- AbbVie (North Chicago, IL)
- …LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Job Title: Director , Program Management Proposed Job Title: Director , Program Management ... and budget. *Establish program strategy and timelines, defining technical and regulatory requirements to support regulatory approvals. *Evaluate contingency… more
- Boehringer Ingelheim (Duluth, GA)
- …benefit programs reflect Boehringer Ingelheim's high regard for our employees. The Executive Director , Animal Health Business Law is the senior legal advisor for ... broad range of legal services, to clients at the CMC level or below as member of the Commercial...depth knowledge of the business, management, and legal and regulatory environment; and the ability to communicate the legal… more
- J&J Family of Companies (Spring House, PA)
- …representative for global project teams, providing toxicology expertise and interfacing with senior management. + Create target risk assessments and develop plans to ... by generating hypotheses and investigative strategies. + Accountable for global regulatory nonclinical documents and health authority responses to support clinical… more
- University of Southern California (Los Angeles, CA)
- …gene therapies and other biological products for internal/external users. The Associate Director of Process Development (cGMP) is responsible for all aspects of ... interactions and activity prioritization. Regularly ensures compliance with all relevant regulatory requirements. + Oversees the implementation of project plans (eg,… more
- J&J Family of Companies (Spring House, PA)
- …Johnson & Johnson Innovative Medicine R&D is recruiting for a Senior Principal Scientist, Nonclinical Safety Lead within Preclinical Sciences and Translational ... a hybrid role and will be located in Spring House, PA. As a Senior Principal Scientist, Nonclinical Safety (NCS) Lead, you will collaborate with innovative and… more